FDA and U.S. Customs Import Rules and Export Traps in 2020

If you are unable to see the message below, [click here to view](. [logo]( [About Us]( [Webinars]( [Seminars]( [Past Seminar Pictures]( [top teaser] 2-day In-person Seminar FDA and U.S. Customs Import Rules and Export Traps in 2020 [Click Here for More Details!]( [bottom teaser] Overview: FDA and the Customs and Border Patrol Service (CBP) have become increasingly sophisticated and equally demanding in the submission of import information and adherence to government procedures. Firms that fail to understand and properly execute an import and export program find their shipments delayed, detained or refused. As of December 2016, FDA and CBP officially implemented the Automated Commercial Environment (ACE) entry filing system. [Read more..](. [divider image] Date & Time Date: December 4th & 5th, 2019 Time: 9:00 AM to 6:00 PM [Download Seminar Brochure]( Venue Washington, DC Courtyard Arlington Crystal City/Reagan National Airport [Download Registration form]( [divider image] [img-160-160]( Casper (Cap) Uldriks ex-FDA Expert and former Associate Center Director of CDRH Casper (Cap) Uldriks, owns Encore Insight LLC, which provides consulting services on FDA Law. He brings over 32 years of experience from the FDA. [top teaser] Reserve your Seat Now! [Enroll Now!]( [bottom teaser] GlobalCompliancePanel 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA. Phone: +1-800-447-9407 Fax: 302 288 6884 [www.globalcompliancepanel.com]( | [Unsubscribe]( Copyright © 2019 GlobalCompliancePanel. All rights reserved. [img 600 290]